4.4 Article

Isolation and Flow Cytometric Analysis of Human Endocervical Gamma Delta T Cells

Journal

JOVE-JOURNAL OF VISUALIZED EXPERIMENTS
Volume -, Issue 120, Pages -

Publisher

JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/55038

Keywords

Immunology; Issue 120; Mucosa; Female reproductive tract; endocervix; intraepithelial lymphocytes; gamma delta T cells; HIV

Funding

  1. National Institute of Allergy and Infectious Diseases and Women's Interagency HIV Infection Study (WIHS) [U01 AI103397]
  2. National Institute of Allergy and Infectious Diseases, National Institutes of Health [P30AI073961]
  3. National Center for Advancing Translational Sciences and the National Institute on Minority Health and Health Disparities, National Institute of Health [UL1TR000460, 1KL2TR000461]
  4. National Institute of Child Health and Human Development, National Institute of Health [K23HD074489]

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The female reproductive tract (FRT) mucosal immune system serves as the first line of defense. Better knowledge of the genital mucosa is therefore essential for understanding pathogenicity of different pathogens including HIV. Gamma delta (GD) T cells are the prototype of 'unconventional' T cells and represent a relatively small subset of T cells defined by their expression of heterodimeric T-cell receptors (TCRs) composed of gamma and delta chains. This sets them apart from the classical and much better known CD4(+) helper T cells and CD8(+) cytotoxic T cells that are defined by alpha-beta TCRs. GD T cells often show tissue-specific localization and are enriched in epithelium. GD T cells orchestrate immune responses in inflammation, tumor surveillance, infectious disease, and autoimmunity. Here, we present a method to reproducibly isolate and analyze human endocervical intraepithelial GD T lymphocytes. We have used endocervical cytobrush samples from women participating in the Women's Interagency HIV Infection Study (WIHS). Knowledge about GD T cells interactions during conditions in which there is an insult to the vaginal mucosal could be applied to any clinical study in which mucosal vulnerability is addressed, including the development of vaginal microbicides. In addition, knowledge about mucosal GD T cell responses has potential for application of GD T cell-based immune therapy in treating infectious diseases.

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